Package 62332-149-08
Brand: olmesartan medoxomil and hydrochlorothiazide
Generic: olmesartan medoxomil and hydrochlorothiazidePackage Facts
Identity
Package NDC
62332-149-08
Digits Only
6233214908
Product NDC
62332-149
Description
80 TABLET in 1 CARTON (62332-149-08)
Marketing
Marketing Status
Brand
olmesartan medoxomil and hydrochlorothiazide
Generic
olmesartan medoxomil and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9a8f34ad-90c6-41a0-b18c-3c9002954bbd", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362332151301", "0362332149308", "0362332150304"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["ca1a0aac-d81d-4c0a-91ea-cb719af772bf"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET in 1 CARTON (62332-149-08)", "package_ndc": "62332-149-08", "marketing_start_date": "20170424"}, {"sample": false, "description": "100 TABLET in 1 CARTON (62332-149-10)", "package_ndc": "62332-149-10", "marketing_start_date": "20170424"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-149-30)", "package_ndc": "62332-149-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62332-149-90)", "package_ndc": "62332-149-90", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-149-91)", "package_ndc": "62332-149-91", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "62332-149_9a8f34ad-90c6-41a0-b18c-3c9002954bbd", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62332-149", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204233", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}